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辐射分解对钇-90标记的Lym-1抗体制剂的影响。

Effects of radiolysis on yttrium-90-labeled Lym-1 antibody preparations.

作者信息

Salako Q A, O'Donnell R T, DeNardo S J

机构信息

Department of Internal Medicine, Molecular Cancer Institute, University of California, Davis, Sacramento 95816, USA.

出版信息

J Nucl Med. 1998 Apr;39(4):667-70.

PMID:9544679
Abstract

UNLABELLED

The physical half-life of 2.6 days and 2.2 MeV beta emissions of 90Y provide excellent properties for radioimmunotherapy applications. However, the clinically useful beta particles may be a source of radiation-induced damage of 90Y-labeled immunoconjugate radiopharmaceuticals during preparation or short-term storage. The stability of 90Y-labeled Lym-1 antibody was studied in standard radiopharmacy conditions to establish a formulation at which radiolysis is not a problem.

METHODS

Lym-1-21T-BAD immunoconjugate intermediate was prepared according to our standard procedure, then labeled with 90Y at 1, 2, 4 and 9.4 mCi/mg Lym-1 using 0.5 M tetramethylammonium acetate, pH 7, labeling buffer. Each mixture was challenged in diethylenetriaminepentaacetic acid to remove nonspecifically bound 90Y. The 90Y-21T-BAD-Lym-1 products were purified by centrifuged molecular sieving column chromatography. The radiochemical purity and immunoreactivity of each preparation was monitored daily by high-performance liquid chromatography (HPLC) and solid-phase radioimmunoassay, respectively, for 3 days. The preparation at 2 mCi/mg was also formulated in 4% (wt/vol) human serum albumin (HSA) overall and at 9.4 mCi/mg in five-fold water, 4 and 10% (wt/vol) HSA overall; all were monitored as above.

RESULTS

The monomeric quality and purity profile of products at 1 and 2 mCi/mg were retained (> or = 80%) as was their immunoreactivity (> or = 75%) over 3 days. The radiochemical purity and immunoreactivity of the product at 4 mCi/mg declined to 65% and 28%, respectively, by 3 days after preparation and in just 48 hr, the product at 9.4 mCi/mg had degraded to 21% in radiochemical purity with only 3% immunoreactivity. The current HPLC data and earlier published chromatographic evidence did not support a compromised radiochemical integrity of 90Y-DOTA complexes by loss of 90Y from the DOTA chelate.

CONCLUSION

Radiolysis of 90Y-labeled antibody preparations did not appear to be a problem at 90Y-21T-BAD-Lym-1 products < or = 2 mCi/mg. Human serum albumin proved to be an effective radioprotectant as the initial 100% immunoreactivity of the product at 2 mCi/mg was retained for 72 hr. The results underscore the need for appropriate formulations and dilutions of clinical doses of 90Y immunopharmaceuticals immediately after manufacture.

摘要

未标记

钇-90的2.6天物理半衰期和2.2兆电子伏特的β发射为放射免疫治疗应用提供了优异的特性。然而,临床上有用的β粒子可能是钇-90标记的免疫缀合物放射性药物在制备或短期储存期间辐射诱导损伤的来源。在标准放射性药物条件下研究了钇-90标记的Lym-1抗体的稳定性,以建立一种放射分解不是问题的制剂。

方法

按照我们的标准程序制备Lym-1-21T-BAD免疫缀合物中间体,然后使用pH值为7的0.5M乙酸四甲基铵标记缓冲液,以1、2、4和9.4毫居里/毫克Lym-1的剂量用钇-90进行标记。每种混合物用二乙烯三胺五乙酸进行处理,以去除非特异性结合的钇-90。钇-90-21T-BAD-Lym-1产物通过离心分子筛柱色谱法进行纯化。通过高效液相色谱(HPLC)和固相放射免疫测定法分别对每种制剂的放射化学纯度和免疫反应性进行3天的每日监测。2毫居里/毫克的制剂还整体配制成4%(重量/体积)的人血清白蛋白(HSA),9.4毫居里/毫克的制剂配制成五倍体积的水、整体为4%和10%(重量/体积)的HSA;所有制剂均按上述方法进行监测。

结果

1和2毫居里/毫克产物的单体质量和纯度分布在3天内保持(≥80%),其免疫反应性也保持(≥75%)。4毫居里/毫克产物的放射化学纯度和免疫反应性在制备后3天分别降至65%和28%,而9.4毫居里/毫克产物在仅48小时内放射化学纯度就降至21%,免疫反应性仅为3%。当前的HPLC数据和早期发表的色谱证据不支持由于DOTA螯合物中钇-90的损失而导致钇-90-DOTA复合物的放射化学完整性受损。

结论

对于钇-90-21T-BAD-Lym-1产物≤2毫居里/毫克,钇-90标记的抗体制剂的放射分解似乎不是问题。人血清白蛋白被证明是一种有效的放射保护剂,因为2毫居里/毫克产物最初的100%免疫反应性保持了72小时。结果强调了在生产后立即对临床剂量的钇-90免疫药物进行适当制剂和稀释的必要性。

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